YUYA [Dr]TAKAKUBO

Dr. YUYA [Dr]TAKAKUBO

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Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2005 in Clinical Orthopaedics and Related Research
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Journal Article
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Y[YUYA [Dr]TAKAKUBO
YUYA [Dr]TAKAKUBO
SFShigenobu Fukushima
Shigenobu Fukushima
TATamon Asano
Tamon Asano
MYMitsunori Yamakawa
Mitsunori Yamakawa
We report a rare case of fibroma of the tendon sheath in the knee. To our knowledge, only three previous cases of fibroma of the tendon sheath in the knee have been reported in the English literature. In our case, T1-weighted magnetic resonance imaging revealed a low intensity signal, T2-weighted magnetic resonance imaging showed a mixed area of high and low signal intensity, and gadolinium-diethylene triaminepentaacetic acid-enhanced magnetic resonance imaging showed faint enhancement at the periphery of the lesion. Magnetic resonance imaging therefore was valid for detection of this intraarticular lesion. The lesion, which was located between the posterior capsule of the left knee and the posterior cruciate ligament, was excised arthroscopically.

27 October 2011 in Journal of Immunology Research
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Journal Article
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Y[YUYA [Dr]TAKAKUBO
YUYA [Dr]TAKAKUBO
YKYrjö T. Konttinen
Yrjö T. Konttinen
Systemic autoimmune and rheumatic diseases (SAIRDs) are thought to develop due to the failure of autoimmune regulation and tolerance. Current therapies, such as biologics, have improved the clinical results of SAIRDs; however, they are not curative treatments. Recently, new discoveries have been made in immune tolerance and inflammation, such as tolerogenic dendritic cells, regulatory T and B cells, Th 17 cells, inflammatory and tolerogenic cytokines, and intracellular signaling pathways. They lay the foundation for the next generation of the therapies beyond the currently used biologic therapies. New drugs should target the core processes involved in disease mechanisms with the aim to attain complete cure combined with safety and low costs compared to the biologic agents. Re-establishment of autoimmune regulation and tolerance in SAIRDs by the end of the current decade should be the final and realistic target.

1 September 2008
Verified
Journal Article
Closed access
Y[YUYA [Dr]TAKAKUBO
YUYA [Dr]TAKAKUBO
MTMichiaki Takagi
Michiaki Takagi
KMKunihiko Maeda
Kunihiko Maeda
YTYasunobu Tamaki
Yasunobu Tamaki
ASAkiko Sasaki
Akiko Sasaki
MYMitsunori Yamakawa
Mitsunori Yamakawa

21 April 2016 in Modern Rheumatology
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Journal Article
Open access
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YHYasuhiko Hirabayashi
Yasuhiko Hirabayashi
YMYasuhiko Munakata
Yasuhiko Munakata
MMMasayuki Miyata
Masayuki Miyata
YUYukitomo Urata
Yukitomo Urata
KSKoichi Saito
Koichi Saito
FGfor the Michinoku Tocilizumab Study Group
for the Michinoku Tocilizumab Study Group
Objective. To evaluate the clinical and structural efficacy of tocilizumab (TCZ) during its long-term administration in patients with rheumatoid arthritis (RA). Methods. In total, 693 patients with RA who started TCZ therapy were followed for 3 years. Clinical efficacy was evaluated by DAS28-ESR and Boolean remission rates in 544 patients. Joint damage was assessed by calculating the modified total Sharp score (mTSS) in 50 patients. Results. When the reason for discontinuation was limited to inadequate response or adverse events, the 1-, 2-, and 3-year continuation rates were 84.0%, 76.8%, and 72.2%, respectively. The mean DAS28-ESR was initially 5.1 and decreased to 2.5 at 6 months and to 2.2 at 36 months. The Boolean remission rate was initially 0.9% and increased to 21.7% at 6 months and to 32.2% at 36 months. The structural remission rates (ΔmTSS/year ≤0.5) were 68.8%, 78.6%, and 88.9% within the first, second, and third years, respectively. The structural remission rate at 3 years (ΔmTSS ≤1.5) was 66.0%, and earlier achievement of swollen joint count (SJC) of 1 or less resulted in better outcomes. Conclusions. TCZ was highly efficacious, and bone destruction was strongly prevented. SJC was an easy-to-use indicator of joint destruction.

11 December 2009 in Modern Rheumatology
Verified
Journal Article
Closed access
Y[YUYA [Dr]TAKAKUBO
YUYA [Dr]TAKAKUBO
MTMichiaki Takagi
Michiaki Takagi
YTYasunobu Tamaki
Yasunobu Tamaki
ASAkiko Sasaki
Akiko Sasaki
HNHaruki Nakano
Haruki Nakano
TOToshihiko Ogino
Toshihiko Ogino
This study aimed to evaluate joint-preserving procedures by a modified Mann method for rheumatoid forefoot deformities and their functional outcomes in the mid-term. Eleven feet in seven patients u...

Y[YUYA [Dr]TAKAKUBO
YUYA [Dr]TAKAKUBO
YWYoshihiro Wanezaki
Yoshihiro Wanezaki
HOHiroharu Oki
Hiroharu Oki
YNYasushi Naganuma
Yasushi Naganuma
JSJunichiro Shibuya
Junichiro Shibuya
MTMichiaki Takagi
Michiaki Takagi
Background: Joint-preserving surgery for the forefoot has been increasingly performed for rheumatoid arthritis (RA). We compared joint-preserving surgeries with resection arthroplasty for RA in the forefoot. Methods: Forefoot surgeries were performed on 62 toes in 42 patients with RA (men: 2; women: 40) between 2002 and 2018. Three groups were compared: PP—31 toes treated with joint-preserving surgery involving the modified Mann method for the big toe and offset osteotomy for lesser toes, PR—15 toes treated with joint-preserving surgery for the big toe and resection arthroplasty for lesser toes, and RR—16 toes treated with resection arthroplasty for all the toes. Results: The PP group had significantly higher mean scores on a scale for RA in the foot and ankle at the latest follow-up than the RR group (86 vs. 75 points; p < 0.05). Hallux valgus (angle > 20°) of the big toe at the latest follow-up recurred in 10 (32%), 9 (60%), and 16 (100%) patients in the PP, PR, and RR groups, respectively. A revision surgery was performed in one patient each in the PP and PR groups. Conclusions: Joint-preserving surgery is superior to resection arthroplasty in preventing function loss and the recurrence of hallux valgus.